A Bayesian adaptive phase I/II clinical trial design with late‐onset competing risk outcomes
From MaRDI portal
Publication:6076490
DOI10.1111/biom.13347zbMath1520.62403WikidataQ98180688 ScholiaQ98180688MaRDI QIDQ6076490
No author found.
Publication date: 17 October 2023
Published in: Biometrics (Search for Journal in Brave)
Cites Work
- Unnamed Item
- Continual Reassessment Method: A Practical Design for Phase 1 Clinical Trials in Cancer
- Dose-Finding Based on Efficacy-Toxicity Trade-Offs
- Bayesian data augmentation dose finding with continual reassessment method and delayed toxicity
- Dose-Finding Designs for HIV Studies
- Continual Reassessment Method for Ordered Groups
- Robust EM Continual Reassessment Method in Oncology Dose Finding
- Design and Analysis of Phase I Clinical Trials
- Bayesian Dose-Finding in Phase I/II Clinical Trials Using Toxicity and Efficacy Odds Ratios
- Patient‐Specific Dose Finding Based on Bivariate Outcomes and Covariates
- The Calculation of Posterior Distributions by Data Augmentation
- A Strategy for Dose-Finding and Safety Monitoring Based on Efficacy and Adverse Outcomes in Phase I/II Clinical Trials
- Sequential Designs for Phase I Clinical Trials with Late‐Onset Toxicities
This page was built for publication: A Bayesian adaptive phase I/II clinical trial design with late‐onset competing risk outcomes